DE102018102663A1 - Verfahren zum herstellen verbesserter quantenpunkt-harzformulierungen - Google Patents
Verfahren zum herstellen verbesserter quantenpunkt-harzformulierungen Download PDFInfo
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- DE102018102663A1 DE102018102663A1 DE102018102663.3A DE102018102663A DE102018102663A1 DE 102018102663 A1 DE102018102663 A1 DE 102018102663A1 DE 102018102663 A DE102018102663 A DE 102018102663A DE 102018102663 A1 DE102018102663 A1 DE 102018102663A1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/02—Use of particular materials as binders, particle coatings or suspension media therefor
- C09K11/025—Use of particular materials as binders, particle coatings or suspension media therefor non-luminescent particle coatings or suspension media
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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- B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
- B01D15/08—Selective adsorption, e.g. chromatography
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
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US10828716B2 (en) * | 2017-06-19 | 2020-11-10 | Lincoln Global, Inc. | Systems and methods for real time, long distance, remote welding |
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Family Cites Families (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6322901B1 (en) | 1997-11-13 | 2001-11-27 | Massachusetts Institute Of Technology | Highly luminescent color-selective nano-crystalline materials |
US7470420B2 (en) | 2000-12-05 | 2008-12-30 | The Regents Of The University Of California | Optical determination of glucose utilizing boronic acid adducts |
WO2003003015A2 (en) | 2001-06-28 | 2003-01-09 | Advanced Research And Technology Institute, Inc. | Methods of preparing multicolor quantum dot tagged beads and conjugates thereof |
US7588828B2 (en) | 2004-04-30 | 2009-09-15 | Nanoco Technologies Limited | Preparation of nanoparticle materials |
JP4072961B2 (ja) | 2004-05-21 | 2008-04-09 | 北海道電力株式会社 | Sog開閉器の系統連系保護機能を備えた制御装置 |
US7557028B1 (en) | 2004-07-28 | 2009-07-07 | Nanosys, Inc. | Process for group III-V semiconductor nanostructure synthesis and compositions made using same |
JP5333777B2 (ja) | 2006-05-22 | 2013-11-06 | ナンヤン テクノロジカル ユニヴァーシティー | 有機メモリデバイス及びその製造方法 |
US9212056B2 (en) | 2006-06-02 | 2015-12-15 | Qd Vision, Inc. | Nanoparticle including multi-functional ligand and method |
WO2008133660A2 (en) | 2006-11-21 | 2008-11-06 | Qd Vision, Inc. | Nanocrystals including a group iiia element and a group va element, method, composition, device and other prodcucts |
KR101018111B1 (ko) | 2008-10-07 | 2011-02-25 | 삼성엘이디 주식회사 | 양자점-금속산화물 복합체, 양자점-금속산화물 복합체의 제조방법 및 양자점-금속산화물 복합체를 포함하는 발광장치 |
GB0821122D0 (en) | 2008-11-19 | 2008-12-24 | Nanoco Technologies Ltd | Semiconductor nanoparticle - based light emitting devices and associated materials and methods |
EP2424941B1 (en) | 2009-05-01 | 2017-05-31 | Nanosys, Inc. | Functionalized matrixes for dispersion of nanostructures |
WO2011031876A1 (en) * | 2009-09-09 | 2011-03-17 | Qd Vision, Inc. | Formulations including nanoparticles |
EP2475717A4 (en) | 2009-09-09 | 2015-01-07 | Qd Vision Inc | PARTICLES WITH NANOPARTICLES, USES THEREOF AND METHOD THEREFOR |
GB0916699D0 (en) | 2009-09-23 | 2009-11-04 | Nanoco Technologies Ltd | Semiconductor nanoparticle-based materials |
JP5940079B2 (ja) | 2010-11-10 | 2016-06-29 | ナノシス・インク. | ディスプレイバックライトユニット及びディスプレイバックライトユニットの形成方法 |
KR101385214B1 (ko) | 2011-12-01 | 2014-04-21 | 주식회사 엘엠에스 | 양자점을 포함하는 조성물 및 이를 이용한 장치 |
CN102585417B (zh) * | 2012-01-04 | 2013-12-25 | 武汉理工大学 | 量子点/聚合物复合一氧化氮荧光探针及其制备方法 |
WO2013122820A1 (en) * | 2012-02-15 | 2013-08-22 | Qd Vision, Inc. | Method of processing quantum dot inks |
EP2852654B1 (en) * | 2012-05-22 | 2017-07-26 | Nanoco Technologies Ltd | Enhancement of quantum yield using highly reflective agents |
TWI596188B (zh) | 2012-07-02 | 2017-08-21 | 奈米系統股份有限公司 | 高度發光奈米結構及其製造方法 |
KR102086712B1 (ko) | 2013-08-14 | 2020-05-15 | 나노코 테크놀로지스 리미티드 | 다상의 수지를 이용한 양자점 막 |
KR101546938B1 (ko) * | 2013-10-08 | 2015-08-24 | 삼성전자주식회사 | 나노 결정 폴리머 복합체 및 그 제조 방법 |
US20170218264A1 (en) | 2014-10-13 | 2017-08-03 | Los Alamos National Security, Llc | Luminescent solar concentrators comprising semiconductor nanocrystals |
KR101686713B1 (ko) * | 2014-12-08 | 2016-12-14 | 엘지전자 주식회사 | 양자점-고분자 복합체의 제조 방법, 양자점-고분자 복합체, 이를 포함하는 광 변환 필름, 백라이트 유닛 및 표시장치 |
JP6277142B2 (ja) | 2015-02-02 | 2018-02-07 | 富士フイルム株式会社 | 機能性複合フィルムおよび量子ドットフィルム |
KR20160097445A (ko) * | 2015-02-06 | 2016-08-18 | 삼성디스플레이 주식회사 | 감광성 수지 조성물 및 표시 패널 |
EP3070109B1 (en) * | 2015-03-16 | 2018-12-05 | Rohm and Haas Electronic Materials LLC | Multilayer polymer composite for encapsulating quantum dots |
CN105504120B (zh) * | 2015-11-30 | 2018-09-21 | 东莞职业技术学院 | 一种双酚芴类丙烯酸树脂及其制备方法、量子点-彩色光敏树脂组合物及其制备方法和应用 |
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2018
- 2018-01-26 US US15/880,879 patent/US10472563B2/en active Active
- 2018-02-01 TW TW107103588A patent/TWI753094B/zh active
- 2018-02-06 JP JP2018019158A patent/JP7129170B2/ja active Active
- 2018-02-06 DE DE102018102663.3A patent/DE102018102663A1/de active Pending
- 2018-02-06 CN CN201810118091.7A patent/CN108440707B/zh active Active
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TW201831437A (zh) | 2018-09-01 |
CN108440707B (zh) | 2021-12-28 |
KR102564151B1 (ko) | 2023-08-04 |
JP2018131607A (ja) | 2018-08-23 |
TWI753094B (zh) | 2022-01-21 |
CN108440707A (zh) | 2018-08-24 |
JP7129170B2 (ja) | 2022-09-01 |
KR20180094788A (ko) | 2018-08-24 |
GB201802439D0 (en) | 2018-03-28 |
GB2564505A (en) | 2019-01-16 |
US10472563B2 (en) | 2019-11-12 |
US20180230377A1 (en) | 2018-08-16 |
GB2564505B (en) | 2022-04-27 |
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